Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.38 (C)
Location

Chromosome 4:54100500 (forward strand) | View in location tab

Co-located

with COSMIC COSM3760660 (C/T)

Most severe consequence
Evidence status

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

Variation displays